What is the event about?

At BSI, we fully understand the difficulties that may be encountered throughout the process to place a medical device on the market, from application to conformity assessment, certification and post-market surveillance. 

Join the Meet the Experts Event for the opportunity to hear from BSI’s world-renowned experts about regulatory and compliance expectations for CE marking and UKCA marking for medical devices. Throughout the day, our experts will provide insights and guidance on the process to place a medical device on the market, clarification on specific requirements, QMS, AI in medical devices and more.

What will participants gain?

  • An understanding of the MDR current state of play, including timelines and updates
  • Learn what good MDR submissions look like and hear common questions raised in the process
  • The opportunity to engage with experts in a Q&A session
  • The chance to network with BSI experts and industry peers

Who should attend?

This event ideally suited for regulatory professionals and consultants in the medical device industry who are navigating QMS, MDR and UKCA regulations to bring products to market. 

Registration

£100 per person (incl. VAT)

Note: In case of cancellation the Eventbrite admin fee will still apply.

All proceeds from the event will be donated to Room to Read, our global charity partner. 

Speakers

Jayanth
Katta
Regulatory Director & Head of Medical Devices Notified Body
Vishal
Thakker
Senior Regulatory Lead & Head of UK Approved Body
Linda
Moon
Head of Global Quality & Accreditation
Matthew 
Crow
Associate Regional Head of Assessment Delivery
John
Clerkin
Global VP Commercial Operations
Damon
Williams
Sales Manager, Medical Devices - UK & Ireland

To find out more about our comprehensive and proven regulatory services, visit our dedicated Medical Devices webpage.

Email: sally.brownbill@bsigroup.com

Phone: +44 345 080 9000

Follow BSI Medical Devices on LinkedIn.